@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_head {
  this: np:hasAssertion dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_assertion ;
    np:hasProvenance dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_provenance ;
    np:hasPublicationInfo dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_provenance a np:Provenance .
  dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_assertion {
  miriam-gene:9370 a ncit:C16612 .
  lld:C3272363 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_provenance {
  dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_assertion dcterms:description "[From a group of DNA samples collected at baseline in a prospective cohort of 14 916 initially healthy American men, we assessed the presence of 5 ADIPOQ genetic variants (rs266729, rs182052, rs822396, rs2241766, and rs1501299) in samples from 600 Caucasian men who subsequently suffered an atherothrombotic event (incident myocardial infarction or ischemic stroke) and from 600 age- and smoking-matched Caucasian men who remained free of reported vascular disease during follow-up (controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP676099.RAKGagf9uPUsQsyyfo1CYipTVPcxU3iV-wxR_yw_rvb08130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:48+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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    prv:usedData dgn-void:disgenetrdf ;
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}